Intellectual Disability
|
0.500 |
GeneticVariation
|
group |
BEFREE |
Alternatively, testing for large-scale MECP2 duplications is recommended for males presenting with mental retardation, an X-linked family history of developmental delay, and a significant proportion of previously described clinical features (particularly a history of recurrent respiratory infections).
|
22123427 |
2012 |
Intellectual Disability
|
0.500 |
GeneticVariation
|
group |
BEFREE |
The aim of the study was: (a) to evaluate the incidence and spectrum of MECP2 mutations in children with RTT and variant MR; (b) to evaluate phenotype-genotype correlations.
|
21982064 |
2012 |
Intellectual Disability
|
0.500 |
GeneticVariation
|
group |
BEFREE |
Rett syndrome (RS), an X-linked neurodevelopmental disorder and the common cause of mental retardation in females, is caused by methyl CpG binding protein 2 (MECP2) gene mutations with a frequency of more than 95% in classical Rett patients.
|
21300488 |
2012 |
Intellectual Disability
|
0.500 |
GeneticVariation
|
group |
BEFREE |
Furthermore, a complex duplication spanning of the MECP2 gene was identified in two brothers who presented with developmental delay and intellectual disability.
|
23055267 |
2012 |
Intellectual Disability
|
0.500 |
GeneticVariation
|
group |
BEFREE |
A case report of Chinese brothers with inherited MECP2-containing duplication: autism and intellectual disability, but not seizures or respiratory infections.
|
22909152 |
2012 |
Intellectual Disability
|
0.500 |
GeneticVariation
|
group |
BEFREE |
In this study we summarize the results of diagnostic testing of 30 patients with Rett syndrome (RTT) or mental retardation of unknown etiology using bidirectional sequencing of the open reading frame of the MECP2 gene.
|
22277191 |
2012 |
Intellectual Disability
|
0.500 |
GeneticVariation
|
group |
BEFREE |
Rett syndrome (RTT), a neurodevelopmental disorder caused by mutations in the X-linked gene encoding methyl-CpG-binding protein2 (MeCP2), is a leading cause of mental retardation in females.
|
21812101 |
2011 |
Intellectual Disability
|
0.500 |
GeneticVariation
|
group |
BEFREE |
This study examined the effects of sedation on auditory brainstem response interpeak latency intervals (i.e., I-III, III-V, and I-V) in two groups: (1) a group with Rett syndrome who were positive for mutations in the MECP2 gene and (2) a group negative for mutations in the MECP2 gene but who were severely to profoundly delayed with other causes of mental retardation.
|
20399386 |
2010 |
Intellectual Disability
|
0.500 |
GeneticVariation
|
group |
BEFREE |
In this study we screened several cohorts of children for CDKL5 mutations, totaling 316 patients, including individuals with a clinical diagnosis of RTT but who were negative for MECP2 mutations (n=102), males with X-linked mental retardation (n=9), patients with West syndrome (n=52), patients with autism (n=59), patients with epileptic encephalopathy (n=33), patients with Aicardi syndrome (n=7) and other patients with intellectual disability with or without seizures (n=54).
|
20397747 |
2010 |
Intellectual Disability
|
0.500 |
GeneticVariation
|
group |
BEFREE |
These findings corroborate other recent reports in the literature and highlight that the overexpression of MECP2 caused by duplications involving this gene is a relatively frequent genetic cause of mental retardation in males, highlighting the importance of MECP2 gene dosage for diagnostic purposes in such cases.
|
19806472 |
2010 |
Intellectual Disability
|
0.500 |
GeneticVariation
|
group |
BEFREE |
This case broadens the phenotypic spectrum of MECP2 abnormalities with consequent implication in diagnosis and genetic counselling of girls with non-syndromic mental retardation.
|
20236124 |
2010 |
Intellectual Disability
|
0.500 |
GeneticVariation
|
group |
BEFREE |
Males with MECP2 mutations present with a broad spectrum of phenotypes ranging from neonatal encephalopathy to nonsyndromic mental retardation (MR).
|
20098342 |
2010 |
Intellectual Disability
|
0.500 |
Biomarker
|
group |
BEFREE |
Multiplex XLMR pedigrees have been reported with only one mutated patient having autism and MR: different X-located MR genes have been shown to be involved (NLGN4, MECP2, OPHN1, ZNF674 and FRAXA) which does not suggest that they could be "autism genes".
|
19160128 |
2009 |
Intellectual Disability
|
0.500 |
GeneticVariation
|
group |
BEFREE |
Mutations in MECP2 cause classic or preserved speech variant Rett syndrome and intellectual disability in females and early demise or marked neurodevelopmental handicap in males.
|
18989701 |
2009 |
Intellectual Disability
|
0.500 |
Biomarker
|
group |
BEFREE |
We scanned methyl-CpG-binding protein 2 gene in 99 Italian patients with pervasive developmental disorder or with nonsyndromal mental retardation.
|
19189931 |
2009 |
Intellectual Disability
|
0.500 |
GeneticVariation
|
group |
BEFREE |
Rett syndrome (RS), a progressive severe neurodevelopmental disorder mainly caused by de novo mutations in the X-chromosomal MeCP2 gene encoding the transcriptional regulator methyl-CpG-binding protein 2, is a leading cause of mental retardation with autistic features in females.
|
19464363 |
2009 |
Intellectual Disability
|
0.500 |
GeneticVariation
|
group |
BEFREE |
In addition, we found three additional MECP2 duplications in 134 male patients with mental retardation and severe, mostly progressive, neurological symptoms, indicating that the mutation frequency could be as high as 2% in this group of patients.
|
18985075 |
2009 |
Intellectual Disability
|
0.500 |
GeneticVariation
|
group |
BEFREE |
A MECP2 mutation in a highly conserved aminoacid causing mental retardation in a male.
|
18678449 |
2009 |
Intellectual Disability
|
0.500 |
GeneticVariation
|
group |
BEFREE |
Furthermore, duplication of the MECP2 genomic region results in mental retardation with speech and social problems.
|
18321864 |
2008 |
Intellectual Disability
|
0.500 |
GeneticVariation
|
group |
BEFREE |
Analysis of highly conserved regions of the 3'UTR of MECP2 gene in patients with clinical diagnosis of Rett syndrome and other disorders associated with mental retardation.
|
18688080 |
2008 |
Intellectual Disability
|
0.500 |
GeneticVariation
|
group |
BEFREE |
Rett syndrome, the most common form of mental retardation in young girls, is due to l mutation of MECP2, encoding a methylated DNA binding protein that translates DNA methylation into gene repression.
|
17965627 |
2008 |
Intellectual Disability
|
0.500 |
GeneticVariation
|
group |
BEFREE |
Different-sized duplications of Xq28, including MECP2, in three males with mental retardation, absent or delayed speech, and recurrent infections.
|
18165974 |
2008 |
Intellectual Disability
|
0.500 |
Biomarker
|
group |
BEFREE |
We propose that disruption of the MeCP2-ATRX interaction leads to pathological changes that contribute to mental retardation.
|
17296936 |
2007 |
Intellectual Disability
|
0.500 |
GeneticVariation
|
group |
BEFREE |
We conclude that in mentally retarded Brazilian males, non-pathogenic variants in the MECP2 gene are more common than actual pathogenic mutations, and therefore alterations in this gene have a weak relationship with mental retardation in males.
|
17084570 |
2007 |
Intellectual Disability
|
0.500 |
GeneticVariation
|
group |
BEFREE |
Mutation screening of the MECP2 gene in a large cohort of 613 fragile-X negative patients with mental retardation.
|
17383248 |
2007 |